ACTRN12619001298101尚未招募2 期
A Phase IIa Study to assess the Efficacy and Safety of ASN-002 alone and in combination with chemotherapy in adult participants with Low-Risk Basal Cell Carcinomas
适应症
试验速览
- 阶段
- 2 期
- 状态
- 尚未招募
- 入组人数
- 84
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Non-randomised trial
- 主要目的
- Treatment
- 盲法
- Open (masking not used)
入排标准
- 年龄范围
- 18 Years 至 o limit（—）
- 性别
- All
入选标准
- •Histologically confirmed low risk nodular and/or superficial basal cell carcinoma 6-20mm in diameter;
- •Acceptable general health;
- •Willingness to have injection therapy followed by surgery;
- •Written informed consent
- •To be eligible, participants must have from 1 to 5 BCCs.
排除标准
- •No or only minimal symptoms;
- •Known or suspected metastatic disease;
- •Pregnant or Lactating females;
- •Clinically active or uncontrolled skin disease;
- •Known sensitivity to ingredients in ASN-002 or chemotherapeutic agent
- •Immunocompromised or receiving immunomodulating agent;
- •Treatment with psoralen plus UVA or UVB therapy within 6 months of the screening visit;
- •Any serious or active medical or psychiatric illness;
- •Recreational or therapeutic drug or alcohol use;
- •Taking any investigational product within 1 month of first dose of ASN-002;
- •History of any immunological disorder
研究者
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